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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2074042Generated: October 31, 2026

Acetone → 5,10,15,20-tetrakis(4-ethynylphenyl)-21H,23H-Porphine

https://huagongshe.com/reaction/2074042

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetoneHCID 180—
ReactantTetrahydrofuranHCID 8028—
ReactantTetrabutylammonium FluorideHCID 2724141—
Reactant5,10,15,20-Tetrakis[4-[2-(trimethylsilyl)ethynyl]phenyl]-21H,23H-porphineHCID 135475294—
SolventChloroform tetrahydrofuranHCID 21956068—
Product5,10,15,20-tetrakis(4-ethynylphenyl)-21H,23H-PorphineHCID 135999243—

Reaction Steps

A solution of 700 mg (0.7 mmol) of protected TEPP (1) obtained above in 500 ml of a chloroform/tetrahydrofuran (THF) mixture (1/1 v/v) was cooled in a bath of liquid nitrogen and acetone to a temperature of between −30 and −50° C., and then a 1 mol/l solution of tetrabutylammonium fluoride (TBAF) in THF (259 mg, 0.99 mmol in 1 ml) was added to the reaction mixture, which was subsequently stirred for 20 hours. The rise in temperature was not controlled. The solvent was subsequently evaporated off and the deprotected porphyrin (2) was obtained in the form of a purple powder (747 mg, 1.05 mmol).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07919046B2
Source datasetuspto-grants-2011_04
ORD IDord-bae87a407f5a4e2f95a0b047939776bb
Source noteuspto-grants-2011_04